A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998531



Internal ID18811381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86044950..86058924hg38UCSC Ensembl
Innerchr4:86966103..86980077hg19UCSC Ensembl
Innerchr4:87185127..87199101hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3813975
hg1913975
hg1813975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5332n100
Supporting Variantsnssv3633905
Samples
Known GenesMAPK10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998531
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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